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[马凡氏综合征中的髋臼突出]

[Acetabular protrusion in Marfan's disease].

作者信息

Clément J L, Lebarbier P, Cahuzac J P, Pasquie M

出版信息

Chir Pediatr. 1985;26(3):153-61.

PMID:4064231
Abstract

The etiologic assessment that had been made on the person of a young girl revealed a protrusio acetabuli which was painful and stiff and the evolution of which was quick, was allowed us to reveal a Marfan's syndrome. On this occasion, we have studied the links between the Marfan's syndrome and the protrusio acetabuli. After having resumed the history of this illness, the author remind us of its main characteristics while insisting upon the orthopedic abnormalities. They define the three steps of a protrusio acetabuli according to the Ruelle and Dubois criteria. For the child, the protrusio acetabuli is said to be primary without any well determined etiology. On the contrary, numerous studies deal with the idiopathic chondrolysis of the hips and describe surprising associations such as scoliosis, kyphosis, deformations of the hands and hereditary characteristics. Twelve observations of the Marfan's syndrome are presented, eleven of which concerning children and one concerning an adult. Among these twenty-four hips, the authors find nineteen protrude hips (80%) which belong to one of the three steps described by Ruelle and Dubois. There is an absence of clinical symptoms in nine cases among the twelve observed and the protrusion is systematically found. In three cases, there existed a functional symptomatology which in two cases, has led us to reveal a Marfan's syndrome. There were great pains of the mechanical type, linked to a limitation of the articular mobility; the radiography revealed an idiopathic chondrolysis of the hips. Moreover, the authors underline the primary importance of the skin-biopsy and of the metacarpal index measure in order to confirm the diagnostic of the Marfan's syndrome. Thus, the protrusio acetabuli appear to be a quasiconstant sign of Marfan's syndrome and has to be included in the long check of the orthopedic abnormalities of such a syndrome. The verification of a deep hip needs to research of the Marfan's syndrome. The primary protrusio acetabuli has to be closely studied, since we have just showed that the Marfan's syndrome was one its rare etiologies known up to now.

摘要

对一名年轻女孩的病因评估显示存在髋臼前突,伴有疼痛和僵硬,且病情发展迅速,这使我们发现了马凡综合征。在此期间,我们研究了马凡综合征与髋臼前突之间的联系。在回顾了这种疾病的病史后,作者提醒我们其主要特征,同时强调了骨科异常情况。他们根据吕埃勒和杜布瓦标准定义了髋臼前突的三个阶段。对于儿童来说,髋臼前突被认为是原发性的,没有任何明确的病因。相反,许多研究涉及髋关节特发性软骨溶解,并描述了一些惊人的关联,如脊柱侧凸、脊柱后凸、手部畸形和遗传特征。本文呈现了12例马凡综合征病例,其中11例为儿童,1例为成人。在这24个髋关节中,作者发现19个髋关节前突(80%),属于吕埃勒和杜布瓦描述的三个阶段之一。在观察的12例中有9例没有临床症状,但系统性地发现了髋臼前突。在3例中,存在功能性症状,其中2例使我们发现了马凡综合征。存在与关节活动受限相关的机械性剧痛;X线检查显示髋关节特发性软骨溶解。此外,作者强调了皮肤活检和掌骨指数测量对于确诊马凡综合征的首要重要性。因此,髋臼前突似乎是马凡综合征的一个几乎恒定的体征,必须纳入对该综合征骨科异常情况的长期检查中。对髋关节深部情况的核查需要排查马凡综合征。原发性髋臼前突必须仔细研究,因为我们刚刚表明马凡综合征是目前已知的其罕见病因之一。

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